Author/Authors :
Shigeyuki Nishimura، نويسنده , , Morie Sekiguchi، نويسنده , , Tatsuji Kano، نويسنده , , Sugao Ishiwata، نويسنده , , Fumihiko Nagasaki، نويسنده , , Toshio Nishide، نويسنده , , Takao Okimoto، نويسنده , , Yasunori Kutsumi، نويسنده , , Yoichi Kuwabara، نويسنده , , Fumimaro Takatsu MD، نويسنده , , Hideo Nishikawa، نويسنده , , Hiroyuki Daida، نويسنده , , Hiroshi Yamaguchi، نويسنده ,
Abstract :
Twenty-five heterozygous familial hypercholesterolemic patients treated with LDL-apheresis and drugs and 11 patients treated with drugs underwent follow-up angiography 2.3 years later. One-hundred thirteen lesions were measured by quantitative angiography. Mean LDL-cholesterol levels during the trial were 140±34 mg/dl in the apheresis group and 170±58 mg/dl (P<0.05) in the control group. The mean changes in minimal lumen diameter of lesions were +0.19±0.30 mm (improved) in the apheresis group (n=76) and −0.44±0.40 mm (worsened) in the control group (n=37) (P<0.0001). When progression and regression were defined as a change in minimal lumen diameter of ±0.67 mm, in the apheresis group, two (8%) patients had progression, 19 (76%) stayed unchanged and four (16%) had regression, but in the control group seven (64%) patients had progression and four (36%) stayed unchanged. The frequency of regression or no change was significantly higher in the apheresis group than in the control group (P<0.004). Intensive cholesterol lowering therapy with LDL-apheresis and lipid lowering drugs can achieve a substantial decrease in LDL-cholesterol levels to induce regression of coronary lesions in familial hypercholesterolemic patients with advanced coronary artery disease.
Keywords :
LDL-apheresis , heterozygous familial hypercholesterolemia , Regression of coronary lesions , coronary artery disease